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Human peroxiredoxin 5 is a peroxynitrite reductase

Authors :
Dubuisson, Marlène
Vander Stricht, Delphine
Clippe, André
Etienne, Florence
Nauser, Thomas
Kissner, Reinhard
Koppenol, Willem H.
Rees, Jean-François
Knoops, Bernard
Source :
FEBS Letters. Jul2004, Vol. 571 Issue 1-3, p161-165. 5p.
Publication Year :
2004

Abstract

Peroxiredoxins are an ubiquitous family of peroxidases widely distributed among prokaryotes and eukaryotes. Peroxiredoxin 5, which is the last discovered mammalian member, was previously shown to reduce peroxides with the use of reducing equivalents derived from thioredoxin. We report here that human peroxiredoxin 5 is also a peroxynitrite reductase. Analysis of peroxiredoxin 5 mutants, in which each of the cysteine residues was mutated, suggests that the nucleophilic attack on the O–O bond of peroxynitrite is performed by the N-terminal peroxidatic Cys47. Moreover, with the use of pulse radiolysis, we show that human peroxiredoxin 5 reduces peroxynitrite with an unequalled high rate constant of (7 ± 3) × 107 M-1 s-1. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
00145793
Volume :
571
Issue :
1-3
Database :
Academic Search Index
Journal :
FEBS Letters
Publication Type :
Academic Journal
Accession number :
13904642
Full Text :
https://doi.org/10.1016/j.febslet.2004.06.080